Pontocerebellar hypoplasia gene panel

A genetic test to identify mutations causing pontocerebellar hypoplasia, a rare neurodegenerative disorder affecting the brain's cerebellum and pons. It helps in the diagnosis of this condition.

Also known asPontocerebellar Hypoplasia Gene Panel Pontocerebellar Hypoplasia Gene Panel

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
Pontocerebellar hypoplasia gene panel includes 1 parameter

  • Specimen

Test code

G778

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Others (fx)Others2 ML

Specimen stability information

Others (Fx)

Specimen rejection criteria

Test run frequency

Every Day TIME - 10:00

Turn around time

28 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

Pontocerebellar hypoplasia gene panel

22000